Palladium Nanoparticles Supported by Carboxylate-Functionalized Porous Organic Polymers for Additive-Free Hydrogen Generation from Formic Acid

被引:26
|
作者
Zhong, Hong [1 ]
Su, Yanqing [1 ,2 ]
Cui, Caiyan [1 ]
Zhou, Feng [1 ]
Li, Xiaoju [2 ]
Wang, Ruihu [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[2] Fujian Normal Univ, Coll Mat Sci & Engn, Fujian Key Lab Polymer Mat, Fuzhou 350007, Fujian, Peoples R China
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2017年 / 5卷 / 09期
基金
中国国家自然科学基金;
关键词
Porous organic polymers; Palladium nanoparticles; Additive free; Hydrogen generation; Sustainable Chemistry; MIYAURA COUPLING REACTION; ROOM-TEMPERATURE; ALLOY NANOPARTICLES; EFFICIENT CATALYST; FREE DEHYDROGENATION; AMBIENT CONDITIONS; STORAGE MATERIALS; PD NANOPARTICLES; ENERGY-STORAGE; CO2; CAPTURE;
D O I
10.1021/acssuschemeng.7b01675
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Facile hydrogen generation from formic acid (FA) is a promising way of hydrogen storage and release in the fuel-cell-based hydrogen economy; the development of efficient heterogeneous catalyst systems for ultrapure H-2 generation from FA in the absence of additives remains a major challenge. Herein, we present a prefunctionalized porous organic polymer (POP) containing 2,6-bis(1,2,3-triazol-4-yl)pyridyl (BTP) units and carboxylate groups. The terdentate BTP and hydrophilic carboxylate are homogeneously incorporated into the host framework of the POP. BTP units with strong chelating ability can effectively stabilize palladium nanoparticles for heterogeneous dehydrogenation of FA, whereas carboxylate not only increases polarity and dispersibility of the catalytic system in aqueous solutions but also functions as basic sites to facilitate the O-H bond dissociation. The catalytic system shows high catalytic activity, excellent stability and superior recyclability in H-2 generation from aqueous FA without any additives.
引用
收藏
页码:8061 / 8069
页数:9
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